CAS 217813-00-8

4,5-difluoro-2-(trimethylsilyl)phenyl triflate

Description:

4,5-Difluoro-2-(trimethylsilyl)phenyl triflate is an organic compound characterized by the presence of a triflate group, which is a highly reactive sulfonate ester, making it a useful electrophile in various chemical reactions. The compound features a phenyl ring substituted with two fluorine atoms at the 4 and 5 positions, enhancing its electron-withdrawing properties and potentially influencing its reactivity and solubility. The trimethylsilyl group attached to the phenyl ring provides steric bulk and can enhance the compound's stability and solubility in organic solvents. This compound is typically used in synthetic organic chemistry, particularly in reactions involving nucleophilic substitutions or as a precursor for the synthesis of more complex molecules. Its unique combination of functional groups allows for diverse applications, including in medicinal chemistry and materials science. As with many triflates, it is important to handle this compound with care due to its reactivity and potential hazards associated with the triflate moiety.

Formula: C₁₀H₁₁F₅O₃SSi

4,5-Difluoro-2-(trimethylsilyl)phenyl trifluoromethanesulfonate

CAS: 217813-00-8

Formula: C₁₀H₁₁F₅O₃SSi

Purity: 98%

Color and Shape: Liquid

Molecular weight: 334.3351

Ref: IN-DA0039GG

4,5-Difluoro-2-(trimethylsilyl)phenyl trifluoromethanesulfonate

CAS: 217813-00-8

4,5-Difluoro-2-(trimethylsilyl)phenyl trifluoromethanesulfonate

Purity: 98%

Molecular weight: 334.34g/mol

Ref: 54-PC111262

4,5-Difluoro-2-(trimethylsilyl)phenyl triflate

CAS: 217813-00-8

4,5-Difluoro-2-(trimethylsilyl)phenyl triflate is an ether that is used for the synthesis of alkenes. It can be used in the synthesis of hydroxyketones, which are important in biomolecular chemistry and pharmaceutical research. 4,5-Difluoro-2-(trimethylsilyl)phenyl triflate can also be used to synthesize arynes and arylation products. This compound is activated with a Lewis acid catalyst and reacts with methide to form an ether linkage. The reaction must be carried out under an inert atmosphere in order to prevent oxidation by air. The product is obtained in high yield and with good functional group compatibility.

Formula: C₁₀H₁₁F₅O₃SSi

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 334.34 g/mol

Ref: 3D-FD176856

4,5-Difluoro-2-(trimethylsilyl)phenyl trifluoromethanesulfonate

CAS: 217813-00-8

Purity: 98%

Molecular weight: 334.3299866

Ref: 10-F781448